A Phase 3b Randomized Double-Blind Placebo-Control Multicenter Evaluation of the Safety and Efficacy of N1539 Administered Preoperatively in Open Unilateral Total Knee Arthroplasty
Brief description of study
Assess the effect of preoperative administration of N1539 on opioid consumption in subjects undergoing open unilateral total knee arthroplasty compared to placebo.
Clinical Study Identifier: s17-01777
ClinicalTrials.gov Identifier: NCTs17-01777
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